Literature DB >> 10841215

Low molecular weight heparin in acute coronary syndrome: evidence for superior or equivalent efficacy compared with unfractionated heparin?

S Kaul1, P K Shah.   

Abstract

This article will review the results of recent clinical trials evaluating low molecular weight heparins (LMWHs) in the management of patients with acute coronary syndromes of unstable angina and non-ST segment elevation MI. Low molecular weight heparins are a new class of anticoagulants that have a number of advantages over unfractionated heparin (UFH) leading to their increasing use for thrombotic vascular disorders. There is convincing evidence that LMWH is more effective than placebo and at least as effective as UFH in reducing the hard end points of death and recurrent myocardial infarction. Convincing evidence for a superior efficacy is mostly limited to the least robust but most prevalent end point of recurrent angina, and benefits appear to be confined predominantly to high-risk patients. The benefits are sustained long-term, but there appears to be no incremental benefit with prolonged treatment. The risk for major bleeding is approximately equivalent to UFH, but minor hemorrhage is clearly increased, especially with vascular instrumentation. The increased bleeding risk together with its long half-life and absence of specific antidote warrants exercising caution when using LMWH with coronary intervention. Low molecular weight heparins have the potential of being cost-neutral or even cost-saving by reducing resource utilization, especially in the setting of aggressive interventional practice pattern. Last, the issue of whether one LMWH preparation is more effective and cost-effective than others remains an open question that can be answered only by direct head-to-head comparison of different LMWH preparations in randomized trials. In conclusion, subcutaneous weight-adjusted LMWH is as effective and safe as intravenous UFH in the management of patients with acute coronary syndromes. The logistic ease of administration without the need for monitoring anticoagulation appears to be the major advantage over UFH.

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Year:  2000        PMID: 10841215     DOI: 10.1016/s0735-1097(00)00648-3

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  10 in total

Review 1.  A guide to drug use during percutaneous coronary intervention.

Authors:  Joseph K Choo; John J Young; Dean J Kereiakes
Journal:  Drugs       Date:  2002       Impact factor: 9.546

2.  A critical review of clinical trials for low-molecular-weight heparin therapy in unstable coronary artery disease.

Authors:  S Husted; R Becker; A Kher
Journal:  Clin Cardiol       Date:  2001-07       Impact factor: 2.882

3.  Low-molecular-weight heparin compared with unfractionated heparin for patients with non-ST-segment elevation acute coronary syndromes treated with glycoprotein IIb/IIIa inhibitors: results from the CRUSADE initiative.

Authors:  Kanwar P Singh; Matthew T Roe; Eric D Peterson; Anita Y Chen; Kenneth W Mahaffey; Shaun G Goodman; Robert A Harrington; Sidney C Smith; W Brian Gibler; E Magnus Ohman; Charles V Pollack
Journal:  J Thromb Thrombolysis       Date:  2006-06       Impact factor: 2.300

Review 4.  Low molecular weight heparin therapy for percutaneous coronary intervention: a practice in evolution.

Authors:  J K Choo; D J Kereiakes
Journal:  J Thromb Thrombolysis       Date:  2001-05       Impact factor: 2.300

5.  Pulmonary delivery of low molecular weight heparins.

Authors:  Tianzhi Yang; Fatima Mustafa; Shuhua Bai; Fakhrul Ahsan
Journal:  Pharm Res       Date:  2004-11       Impact factor: 4.200

6.  Heparin in interventional radiology: a therapy in evolution.

Authors:  Stuart B Resnick; Stephanie H Resnick; Joshua L Weintraub; Nishita Kothary
Journal:  Semin Intervent Radiol       Date:  2005-06       Impact factor: 1.513

7.  Development of a dosage strategy in patients receiving enoxaparin by continuous intravenous infusion using modelling and simulation.

Authors:  Yan Feng; Bruce Green; Stephen B Duffull; Sandra L Kane-Gill; Mary B Bobek; Robert R Bies
Journal:  Br J Clin Pharmacol       Date:  2006-08       Impact factor: 4.335

8.  Complexation of a poly-L-arginine with low molecular weight heparin enhances pulmonary absorption of the drug.

Authors:  Amit Rawat; Tianzhi Yang; Alamdar Hussain; Fakhrul Ahsan
Journal:  Pharm Res       Date:  2007-10-23       Impact factor: 4.200

Review 9.  Enoxaparin: an update of its clinical use in the management of acute coronary syndromes.

Authors:  Tim Ibbotson; Karen L Goa
Journal:  Drugs       Date:  2002       Impact factor: 9.546

Review 10.  Heparin versus placebo for non-ST elevation acute coronary syndromes.

Authors:  Carlos A Andrade-Castellanos; Luis E Colunga-Lozano; Netzahualpilli Delgado-Figueroa; Kirk Magee
Journal:  Cochrane Database Syst Rev       Date:  2014-06-27
  10 in total

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